Alcoscrub Foam by Erie Scientific, LLC ALCOSCRUB FOAM liquid

Alcoscrub Foam by

Drug Labeling and Warnings

Alcoscrub Foam by is a Otc medication manufactured, distributed, or labeled by Erie Scientific, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Ethyl Alcohol 62% v/v

INACTIVE INGREDIENT

DEA-C8-18 Perfluoroalkylethyl Phosphate, Glycerin, Water

DOSAGE & ADMINISTRATION

Use as part of your daily cleaning routine. Apply a small amount to palm. Rub product into hands and allow to dry.

PURPOSE

Antiseptic Cleanser. Effective in destroying certain bacteria and removing impurities to provide antiseptic cleansing.

INDICATIONS & USAGE

Antiseptic cleanser. Use as part of your daily cleaning routine.

Flammable. Keep away from open flame and sources of heat. Avoid contact with eyes.

Discontinue use and ask a health practitioner if irritation develops. If swallowed seek medical help or contact Posion Control immediately. Keep out of reach of children.

KEEP OUT OF REACH OF CHILDREN

If swallowed seek medical help or contact Posion Control immediately.

WARNINGS

For external use only.

Flammable. Keep away from open flame and sources of heat.

Avoid contact with eyes. If contact occurs, flush eyes with water.

Discontinue use and ask a health practitioner if irritation develops.

If swallowed seek medical help or contact Posion Control immediately.

Keep out of reach of children.

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALCOSCRUB FOAM 
alcoscrub foam liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55863-431
Route of Administration	Topical

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	1 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE (UNII: 4J55VM509S)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55863-431-02	50 mL in 1 BOTTLE
2	NDC: 55863-431-32	950 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	01/12/2006

Labeler - Erie Scientific, LLC (361605223)